Canonical Allele Identifier: CA2687200476
Gene: PRKDC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47852742del , CM000670.2:g.47852742del GRCh38
NC_000008.10:g.48765303del , CM000670.1:g.48765303del GRCh37
NC_000008.9:g.48927856del NCBI36
NG_023435.1:g.112442del , LRG_162:g.112442del

Transcript Alleles

HGVS Amino-acid change
ENST00000314191.7:c.6936del MANE Select ENSP00000313420.3:p.Tyr2312Ter
ENST00000314191.6:c.6936del ENSP00000313420.3:p.Tyr2312Ter
ENST00000338368.7:c.6936del ENSP00000345182.4:p.Tyr2312Ter
NM_001081640.1:c.6936del NP_001075109.1:p.Tyr2312Ter
NM_006904.6:c.6936del , LRG_162t1:c.6936del NP_008835.5:p.Tyr2312Ter
XM_011517567.1:c.6936del XP_011515869.1:p.Tyr2312Ter
XM_011517568.1:c.6936del XP_011515870.1:p.Tyr2312Ter
NM_001081640.2:c.6936del NP_001075109.1:p.Tyr2312Ter
NM_006904.7:c.6936del MANE Select NP_008835.5:p.Tyr2312Ter